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Review

HPLC Separation of Diastereomers: Chiral Molecular Tools Useful for the Preparation of Enantiopure Compounds and Simultaneous Determination of Their Absolute Configurations

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba, Sendai 980-8577, Japan
Received: 20 August 2016 / Accepted: 26 September 2016 / Published: 4 October 2016
To obtain enantiopure compounds, the so-called chiral high performance liquid chromatography (HPLC) method, i.e., HPLC using a chiral stationary phase, is very useful, as reviewed in the present Special Issue. On the other hand, normal HPLC (on silica gel) separation of diastereomers is also useful for the preparation of enantiopure compounds and also for the simultaneous determination of their absolute configurations (ACs). The author and coworkers have developed some chiral molecular tools, e.g., camphorsultam dichlorophthalic acid (CSDP acid), 2-methoxy-2-(1-naphthyl)propionic acid (MαNP acid), and others suitable for this purpose. For example, a racemic alcohol is esterified with (S)-(+)-MαNP acid, yielding diastereomeric esters, which are easily separable by HPLC on silica gel. The ACs of the obtained enantiopure MαNP esters can be determined by the 1H-NMR diamagnetic anisotropy method. In addition, MαNP or CSDP esters have a high probability of giving single crystals suitable for X-ray crystallography. From the X-ray Oak Ridge thermal ellipsoid plot (ORTEP) drawing, the AC of the alcohol part can be unambiguously determined because the AC of the acid part is already known. The hydrolysis of MαNP or CSDP esters yields enantiopure alcohols with the established ACs. The mechanism and application examples of these methods are explained. View Full-Text
Keywords: chiral molecule; absolute configuration; diastereomers; HPLC separation on silica gel; 1H-NMR diamagnetic anisotropy; X-ray crystallography; internal reference of absolute configuration chiral molecule; absolute configuration; diastereomers; HPLC separation on silica gel; 1H-NMR diamagnetic anisotropy; X-ray crystallography; internal reference of absolute configuration
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MDPI and ACS Style

Harada, N. HPLC Separation of Diastereomers: Chiral Molecular Tools Useful for the Preparation of Enantiopure Compounds and Simultaneous Determination of Their Absolute Configurations. Molecules 2016, 21, 1328. https://0-doi-org.brum.beds.ac.uk/10.3390/molecules21101328

AMA Style

Harada N. HPLC Separation of Diastereomers: Chiral Molecular Tools Useful for the Preparation of Enantiopure Compounds and Simultaneous Determination of Their Absolute Configurations. Molecules. 2016; 21(10):1328. https://0-doi-org.brum.beds.ac.uk/10.3390/molecules21101328

Chicago/Turabian Style

Harada, Nobuyuki. 2016. "HPLC Separation of Diastereomers: Chiral Molecular Tools Useful for the Preparation of Enantiopure Compounds and Simultaneous Determination of Their Absolute Configurations" Molecules 21, no. 10: 1328. https://0-doi-org.brum.beds.ac.uk/10.3390/molecules21101328

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